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Genotype
Genotype
Quantitative genetics of larval life-history traits in Rana temporaria in different environmental conditions
Genetics / Geography / Population Genetics / Quantitative Genetics / Animals / Temperature / Phenotype / GENETICAL / Genotype / Environmental Conditions / Time Factors / Reproducibility of Results / Genetic variation / Environment / Rana temporaria / Temperature / Phenotype / GENETICAL / Genotype / Environmental Conditions / Time Factors / Reproducibility of Results / Genetic variation / Environment / Rana temporaria
Intestinal PTGS2 mRNA Levels, PTGS2 Gene Polymorphisms, and Colorectal Carcinogenesis
Multidisciplinary / Humans / Female / Male / PLoS one / Aged / Intestines / Middle Aged / Carcinogenesis / Genotype / Adenoma / Adenocarcinoma / Case Control Studies / Aged / Intestines / Middle Aged / Carcinogenesis / Genotype / Adenoma / Adenocarcinoma / Case Control Studies
Genetic Variants in Nuclear-Encoded Mitochondrial Genes Influence AIDS Progression
Genetics / Mitochondria / Multidisciplinary / Mitochondrial DNA / Humans / Female / Male / PLoS one / Mitochondrial Genome / Cell nucleus / Genotype / Redox Regulation / Single Nucleotide Polymorphism / Adverse Event / European Continental Ancestry Group / Genetic variation / Disease Progression / Protein Transport / Cohort Studies / Acquired immunodeficiency syndrome / Female / Male / PLoS one / Mitochondrial Genome / Cell nucleus / Genotype / Redox Regulation / Single Nucleotide Polymorphism / Adverse Event / European Continental Ancestry Group / Genetic variation / Disease Progression / Protein Transport / Cohort Studies / Acquired immunodeficiency syndrome
Genes expressed in dental enamel development are associated with molar-incisor hypomineralization
Zoology / Dentistry / Biomedical Engineering / Brazil / Turkey / Gene expression / Humans / Female / Male / Young Adult / Proteins / Risk factors / Amelogenesis / Amelogenin / Genotype / Adult / Genetic variation / Risk Factors / Streptococcus mutans / Dental Enamel Hypoplasia / Extracellular Matrix Proteins / Case Control Studies / Gene expression / Humans / Female / Male / Young Adult / Proteins / Risk factors / Amelogenesis / Amelogenin / Genotype / Adult / Genetic variation / Risk Factors / Streptococcus mutans / Dental Enamel Hypoplasia / Extracellular Matrix Proteins / Case Control Studies
Coenzyme Q supports distinct developmental processes in Caenorhabditis elegans
Caenorhabditis elegans / Aging / Fertility / Longevity / Animals / Life Cycle / Phenotype / Clinical Sciences / Genotype / Larva / Embryos / Life Span / Gonads / Coenzyme Q / Embryo Development / Life Cycle / Phenotype / Clinical Sciences / Genotype / Larva / Embryos / Life Span / Gonads / Coenzyme Q / Embryo Development
HLA-G protein expression as a potential immune escape mechanism in classical Hodgkin’s lymphoma
Immunology / Immune response / Population Genetics / Immunohistochemistry / Adolescent / Humans / Child / Natural Killer cells / Female / Male / Clinical Sciences / Tissue / Aged / Middle Aged / Epstein-Barr virus / Genotype / Adult / Major histocompatibility complex / Protein Expression / natural killer (NK) cell / G protein / Genetic Markers / NK Cell / MHC class I / Hodgkin disease / Humans / Child / Natural Killer cells / Female / Male / Clinical Sciences / Tissue / Aged / Middle Aged / Epstein-Barr virus / Genotype / Adult / Major histocompatibility complex / Protein Expression / natural killer (NK) cell / G protein / Genetic Markers / NK Cell / MHC class I / Hodgkin disease
Explaining variability in ciclosporin exposure in adult kidney transplant recipients
Genetics / Kidney transplantation / Survival Analysis / Therapeutic drug monitoring / Humans / Female / Blood sampling / Male / P-glycoprotein / Cyclosporine / Prednisolone / Aged / Middle Aged / Genotype / Kidney Transplant / Adult / Genetic Polymorphism / Body Weight / Bovine Serum Albumin / Genetic Variability / Female / Blood sampling / Male / P-glycoprotein / Cyclosporine / Prednisolone / Aged / Middle Aged / Genotype / Kidney Transplant / Adult / Genetic Polymorphism / Body Weight / Bovine Serum Albumin / Genetic Variability
Genetic Variants in Nuclear-Encoded Mitochondrial Genes Influence AIDS Progression
Genetics / Mitochondria / Multidisciplinary / Mitochondrial DNA / Humans / Female / Male / PLoS one / Mitochondrial Genome / Cell nucleus / Genotype / Redox Regulation / Single Nucleotide Polymorphism / Adverse Event / European Continental Ancestry Group / Genetic variation / Disease Progression / Protein Transport / Cohort Studies / Acquired immunodeficiency syndrome / Female / Male / PLoS one / Mitochondrial Genome / Cell nucleus / Genotype / Redox Regulation / Single Nucleotide Polymorphism / Adverse Event / European Continental Ancestry Group / Genetic variation / Disease Progression / Protein Transport / Cohort Studies / Acquired immunodeficiency syndrome
Genetic variation in aldosterone synthase predicts plasma glucose levels
Multidisciplinary / Humans / Blood Glucose / Insulin / Diabetes mellitus / Female / Male / Middle Aged / Genotype / Adult / Genetic variation / Base Sequence / Glucose Tolerance Test / Female / Male / Middle Aged / Genotype / Adult / Genetic variation / Base Sequence / Glucose Tolerance Test
Porphyria cutanea tarda in an HCV-positive liver transplant patient: a case report
Treatment Outcome / Biopsy / Humans / Liver Cirrhosis / Male / Liver Transplantation / Recurrence / Genotype / Adult / Combination drug therapy / Liver Failure / Chloroquine / Recombinant Proteins / Polyethylene Glycols / Ribavirin / Antiviral Agents / Hemolysis / Interferon Alpha / Liver Transplantation / Recurrence / Genotype / Adult / Combination drug therapy / Liver Failure / Chloroquine / Recombinant Proteins / Polyethylene Glycols / Ribavirin / Antiviral Agents / Hemolysis / Interferon Alpha
Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism
Genetics / Cognitive Science / Pediatrics / Transcranial Magnetic Stimulation / Neurogenetics / Intellectual Disability / Subthalamic Nucleus / DNA / Humans / Mutation / Female / Clinical Genetics / Inborn errors of metabolism / Male / Infant / Follow-up studies / Differential Diagnosis / Phenotype / Child Neurology / Clinical Sciences / Mouse Model / Genotype / Adult / Globus Pallidus / Sleep Disorder / Status Epilepticus / Base Sequence / NAD / Lymphocytes / Neurosciences / Gamma-Aminobutyric Acid / Ketogenic diet / Intellectual Disability / Subthalamic Nucleus / DNA / Humans / Mutation / Female / Clinical Genetics / Inborn errors of metabolism / Male / Infant / Follow-up studies / Differential Diagnosis / Phenotype / Child Neurology / Clinical Sciences / Mouse Model / Genotype / Adult / Globus Pallidus / Sleep Disorder / Status Epilepticus / Base Sequence / NAD / Lymphocytes / Neurosciences / Gamma-Aminobutyric Acid / Ketogenic diet
Clinical and Genetic Heterogeneity in Familial Temporal Lobe Epilepsy
Humans / Temporal Lobe Epilepsy / Phenotype / Genetic linkage analysis / Epilepsia / Clinical Sciences / Genotype / Chromosome segregation / Genetic variation / Neurosciences / Clinical Sciences / Genotype / Chromosome segregation / Genetic variation / Neurosciences
Interacción entre los polimorfismos del receptor ß1 y ß2 adrenérgico como predictor de riesgo de insuficiencia cardiaca crónica
Heart Failure / Humans / Chronic Disease / Female / Male / Young Adult / Risk factors / Aged / Middle Aged / Genotype / Myocardial Infarction / Adult / Risk Factors / Case Control Studies / Young Adult / Risk factors / Aged / Middle Aged / Genotype / Myocardial Infarction / Adult / Risk Factors / Case Control Studies
N-acetyltransferase 2 polymorphism in sporadic Parkinson\'s disease in a Polish population
Polymorphism / Poland / Humans / DNA Extraction / Polymerase Chain Reaction / Statistical Significance / Arylamine N-acetyltransferase / European / Aged / Middle Aged / Genotype / Adult / Acetylation / Parkinson Disease / Control Group / Statistical Significance / Arylamine N-acetyltransferase / European / Aged / Middle Aged / Genotype / Adult / Acetylation / Parkinson Disease / Control Group
Clinical and Genetic Heterogeneity in Familial Temporal Lobe Epilepsy
Humans / Temporal Lobe Epilepsy / Phenotype / Genetic linkage analysis / Epilepsia / Clinical Sciences / Genotype / Chromosome segregation / Genetic variation / Neurosciences / Clinical Sciences / Genotype / Chromosome segregation / Genetic variation / Neurosciences
Increased Expression of Catalase and Superoxide Dismutase 2 Reduces Cone Cell Death in Retinitis Pigmentosa
Technology / Genetic Engineering / Biological Sciences / Molecular / Mice / Retinitis pigmentosa / Animals / Cell Death / Retina / Catalase / Superoxide Dismutase / Genotype / Oxidative Damage / Molecular Targeted Therapy / Enzyme Linked Immunosorbent Assay / Superoxides / Immunoblotting / Retinitis pigmentosa / Animals / Cell Death / Retina / Catalase / Superoxide Dismutase / Genotype / Oxidative Damage / Molecular Targeted Therapy / Enzyme Linked Immunosorbent Assay / Superoxides / Immunoblotting
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